薗头偶联反应
双金属片
芳基
光化学
卤化物
催化作用
光催化
金属
化学
偶联反应
多相催化
钯
材料科学
无机化学
有机化学
烷基
作者
Munusamy Shanmugam,Arunachalam Sagadevan,Vaibhav Pramod Charpe,V. Kishore Kumar Pampana,Kuo Chu Hwang
出处
期刊:Chemsuschem
[Wiley]
日期:2019-09-02
卷期号:13 (2): 287-292
被引量:27
标识
DOI:10.1002/cssc.201901813
摘要
Herein the first visible-light-activated Sonogashira C-C coupling reaction at room temperature catalyzed by single-metal heterogeneous Cu2 O truncated nanocubes (Cu2 O TNCs) was developed. A wide variety of aryl halides and terminal alkynes worked well in this recyclable heterogeneous photochemical process to form the corresponding Sonogashira C-C coupling products in good yields. Mechanistic control studies indicated that CO2 enhances the formation of light-absorbing heterogeneous surface-bound CuI -phenylacetylide (λmax =472 nm), which further undergoes single-electron transfer with aryl iodides/bromides to enable Sonogashira C sp2 -Csp bond formation. In contrast to literature-reported bimetallic TiO2 -containing nanoparticles as photocatalyst, this work avoided the need of cocatalysis by TiO2 . Single-metal CuI in Cu2 O TNCs was solely responsible for the observed C sp2 -Csp coupling reactions under CO2 atmosphere.
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